Scott Ritchey Research Center, College of Veterinary Medicine, Auburn University, AL, USA.
Cancer Biol Ther. 2011 Apr 1;11(7):651-8. doi: 10.4161/cbt.11.7.14690.
Recombinant adenovirus vectors (Ad) have been recognized as effective in vivo gene delivery vehicles and utilized as gene therapy agents for a number of cancers. The elucidation of viral entry mechanisms has allowed the development of recombinant vectors that exploit existing cell surface receptors to achieve entry into the cell. B lymphocytes are normally resistant to infection by adenovirus 5, likely due to the lack of the Coxsackie and Adenovirus receptor (CAR). Using reverse-transcriptase PCR and flow cytometry, the CD40 receptor has been shown to be expressed on many lymphoma cells. We exploited this finding to develop a gene therapy strategy for treatment of canine B cell lymphoma. Ad5 was targeted to cells expressing CD40 via CD40 ligand (CD40L) and was effective in infecting CD40-expressing control cells; however, both primary canine lymphoma cells and cell lines demonstrated limited evidence of transduction. Following receptor binding, adenovirus entry into cells may require interaction with α(v)β(3/5) integrins; we demonstrate that canine lymphoma cells are deficient in these integrins. Reduced α(v)β(3) integrin expression may render these cells incapable of internalizing Ad vectors. Thus, any viral targeting approaches for treatment of canine lymphoma must also take into account the potential lack of internalization signals.
重组腺病毒载体(Ad)已被认为是有效的体内基因传递载体,并被用作多种癌症的基因治疗剂。病毒进入机制的阐明允许开发利用现有细胞表面受体进入细胞的重组载体。B 淋巴细胞通常对腺病毒 5 感染具有抗性,这可能是由于缺乏柯萨奇病毒和腺病毒受体(CAR)。通过逆转录酶 PCR 和流式细胞术,已经证明 CD40 受体在许多淋巴瘤细胞上表达。我们利用这一发现开发了一种针对犬 B 细胞淋巴瘤的基因治疗策略。Ad5 通过 CD40 配体(CD40L)靶向表达 CD40 的细胞,并有效地感染表达 CD40 的对照细胞;然而,原发性犬淋巴瘤细胞和细胞系都表现出转导的证据有限。在受体结合后,腺病毒进入细胞可能需要与α(v)β(3/5)整合素相互作用;我们证明犬淋巴瘤细胞缺乏这些整合素。α(v)β(3)整合素表达减少可能使这些细胞无法内化 Ad 载体。因此,任何用于治疗犬淋巴瘤的病毒靶向方法都必须考虑到缺乏内化信号的可能性。